Canonical Allele Identifier: CA371586252

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220477T>C (hg19) ; chr8:g.102208249T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208249T>C , CM000670.2:g.102208249T>C	GRCh38
NC_000008.10:g.103220477T>C , CM000670.1:g.103220477T>C	GRCh37
NC_000008.9:g.103289653T>C	NCBI36
NG_016617.1:g.35870A>G , LRG_788:g.35870A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.940A>G MANE Select	ENSP00000251810.3:p.Asn314Asp
ENST00000251810.7:c.940A>G	ENSP00000251810.3:p.Asn314Asp
ENST00000395910.6:n.327A>G
ENST00000395912.6:c.784A>G	ENSP00000379248.2:p.Asn262Asp
ENST00000519317.5:c.304A>G	ENSP00000430641.1:p.Asn102Asp
ENST00000519962.5:c.85A>G	ENSP00000429140.1:p.Asn29Asp
ENST00000522368.5:c.1109A>G
ENST00000522394.1:c.273A>G	ENSP00000429578.1:n.273A>G
ENST00000621845.1:c.778A>G	ENSP00000484318.1:p.Asn260Asp
NM_001172477.1:c.1156A>G , LRG_788t1:c.1156A>G	NP_001165948.1:p.Asn386Asp
NM_001172478.1:c.784A>G	NP_001165949.1:p.Asn262Asp
NM_015713.4:c.940A>G , LRG_788t2:c.940A>G	NP_056528.2:p.Asn314Asp
NM_001172478.2:c.784A>G	NP_001165949.1:p.Asn262Asp
NM_015713.5:c.940A>G MANE Select	NP_056528.2:p.Asn314Asp